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Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ
Abstract
A rapid, direct method for screening single plaques of λgt recombinant phage is described. The method allows at least 10 6 clones to be screened per day and simplifies physical containment of recombinants.
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Cited by
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
Feinberg, A. P., & Vogelstein, B. (1983) · Analytical Biochemistry · doi:10.1016/0003-2697(83)90418-9 · Cited by 24,887
Positional cloning of the mouse obese gene and its human homologue
Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419
Ullrich, A., Coussens, L., Hayflick, J. S., Dull, T. J., Gray, A., Tam, A. W., Lee, J., Yarden, Y., Libermann, T. A., Schlessinger, J., et al. (1984) · Nature · doi:10.1038/309418a0 · Cited by 2,752
Koenig, M., Hoffman, E. P., Bertelson, C. J., Monaco, A. P., Feener, C., & Kunkel, L. M. (1987) · Cell · doi:10.1016/0092-8674(87)90504-6 · Cited by 2,411
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
Geissler, E. N., Ryan, M. A., & Housman, D. E. (1988) · Cell · doi:10.1016/0092-8674(88)90020-7 · Cited by 1,287
Metadata
- Authors
- Benton, W. D., & Davis, R. W.
- Venue
- Science
- Published
- 1977-04-08
- Volume
- 196
- Issue
- 4286
- Pages
- 180-182
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1995420892
- Cited by
- 4,595
- References
- 0
- FWCI
- 129.38
- Type
- journal article
- Language
- en
- Open access
- closed
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- Benton, W. D., & Davis, R. W. (1977). Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ. Science. https://doi.org/10.1126/science.322279
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.